Fluorescence-based nanofluidic biosensor platform for real-time measurement of protein binding kinetics

Figure 122 : Spectres de masse d’ions secondaires positifs entre 0 < m/z < 200 pour la sélection « Comète » (les 494 spectres de masse sélectionnés sur 25 particules) et

One-shot kinetic assay in nanofluidic sensors with integrated concentration gradient generator With an optimized flow velocity of the injected solutions at the inlet reservoirs,

Whereas, under the current regime of private international law, it is the insurer who hesitates to provide cross border services, the policyholder would be reluctant to

injection of such mutated Y29F or K33A ACBP/DBI recombinant proteins induced a similar hyperphagic response as did the WT protein (Fig. 1 a), indicating that appetite stimulation

a high temperature (infinite in lattice mortels) to a temperature close to the folding transition temperature. The approach to the native state is then monitored using

For this reason we have started an analysis of the interactions between Biotin and Streptavidin using the tool of fluorescence correlation spectroscopy (FCS), which is able to

We have previously observed that HMGB1 binds with extremely high affinity to a novel DNA structure, hemicatenated DNA loops (hcDNA), in which double-stranded DNA

In the present study, we employ a real-time approach to study the dynamics of the interactions between charged membranes and oppositely charged PE molecules, and monitored by light